A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616926



Internal ID21565231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85817544..85817544hg38UCSC Ensembl
chr2:86044667..86044667hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115627
SamplesHG02587
Known GenesLOC284950
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616926
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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